The following data is part of a premarket notification filed by Intuitive Surgical with the FDA for Sureform 45, Sureform 45 Reloads.
Device ID | K183224 |
510k Number | K183224 |
Device Name: | SureForm 45, SureForm 45 Reloads |
Classification | System, Surgical, Computer Controlled Instrument |
Applicant | Intuitive Surgical 1266 Kifer Road Sunnyvale, CA 94086 |
Contact | Nadine Nasr |
Correspondent | Nadine Nasr Intuitive Surgical 1266 Kifer Road Sunnyvale, CA 94086 |
Product Code | NAY |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-11-20 |
Decision Date | 2019-01-18 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10886874117580 | K183224 | 000 |
10886874117122 | K183224 | 000 |
10886874117115 | K183224 | 000 |
10886874117092 | K183224 | 000 |
10886874117085 | K183224 | 000 |